About: Guy Lloyd-Jones

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

British organic chemist

Attributes	Values
rdf:type	Item
field of work	wds:Q5622427-BEDFB735-ED62-483B-B656-65AC78955458
field of work	chemistry
owl:sameAs	Guy Lloyd-Jones
description	scheikundige (nl) British academic (en-ca) British academic (en-gb) académico británico (es) أكاديمي بريطاني (ar) British organic chemist (en)
rdfs:label	Guy Lloyd-Jones (en) Guy Lloyd-Jones (es) Guy Lloyd-Jones (fr) Guy Lloyd-Jones (nl) Guy Lloyd-Jones (sl) Guy Lloyd-Jones (sq) Guy Lloyd-Jones (tr) Guy Lloyd-Jones (ast)
skos:prefLabel	Guy Lloyd-Jones (en) Guy Lloyd-Jones (es) Guy Lloyd-Jones (fr) Guy Lloyd-Jones (nl) Guy Lloyd-Jones (sl) Guy Lloyd-Jones (sq) Guy Lloyd-Jones (tr) Guy Lloyd-Jones (ast)
name	Guy Lloyd-Jones (en) Guy Lloyd-Jones (es) Guy Lloyd-Jones (fr) Guy Lloyd-Jones (nl) Guy Lloyd-Jones (sl) Guy Lloyd-Jones (sq) Guy Lloyd-Jones (tr) Guy Lloyd-Jones (ast)
Freebase ID	wds:Q5622427-F2487D12-8A52-4D1D-9838-05D83C006B3E
Freebase ID	/m/0n_8wwh
Scopus author ID	wds:Q5622427-55d0fe15-416e-3f59-b1b2-2416bb0dbde5
Scopus author ID	7005241494
given name	wds:Q5622427-68B326AA-8575-42EB-A37F-9ED4900FE7C5
given name	Guy
instance of	wds:Q5622427-62B7E094-9ADC-4FA1-A508-BB52C9A3FD3C
instance of	Homo sapiens
award received	wds:Q5622427-3ab3f1be-409f-f275-49b4-64ada89eae63 wds:Q5622427-4E65F0FA-75EA-4B20-B3EA-B7253CEC88BF wds:Q5622427-7EEE6E4A-1FDF-45EB-A6B3-FB70212A7CC8 wds:Q5622427-A8316F69-C23E-4525-917A-AC473F9B0AB0
award received	Hickinbottom Award Fellow of the Royal Society Tilden Prize Corday-Morgan Prize
Fellow of the Royal Society ID	wds:Q5622427-C27F02BE-8976-459B-A52A-C5670970AEA1
Fellow of the Royal Society ID	11829
Academic Tree ID	wds:Q5622427-ca908a62-42fa-dba8-1600-fb4c61e20819
Academic Tree ID	79374
Google Scholar author ID	wds:Q5622427-5b70639b-4b95-1327-a179-931dc8c818e2
Google Scholar author ID	8SGYLsUAAAAJ
skos:altLabel	Guy Charles Lloyd-Jones (en)
occupation	wds:Q5622427-5FF17D33-AFA2-4D0E-A506-48D268CD7B41
employer	wds:Q5622427-1E807BC0-1CAF-44DF-BB28-A280BC39A8FB wds:Q5622427-55F2ECDA-18F3-4142-AEBD-1ACD2AFDFEBE
place of birth	wds:Q5622427-34321465-D1BF-4470-AC52-D8033A48CAF9
sex or gender	wds:Q5622427-0963B489-BF04-4B95-A112-152007599F8A
member of	wds:Q5622427-A839A9EC-1AC9-435C-A030-DD2DC567BC2C
Who's Who UK ID	wds:Q5622427-7fde2cb7-4422-b003-7c76-4ff073e3a84f
date of birth	wds:Q5622427-58340534-22AF-4794-B74F-99CB617C37DD
educated at	wds:Q5622427-AF2DDEDC-8BE9-41A9-B3AE-1E4C771C621A wds:Q5622427-F4C59AA9-E958-429C-9096-A948B9BB0744
family name	wds:Q5622427-C9952E60-F762-4350-BD81-5AE04665ECD1
occupation	chemist
employer	University of Bristol University of Edinburgh
place of birth	London (Samian Ware Discovery Site)
sex or gender	male
member of	Royal Society
Who's Who UK ID	U267358
date of birth	1966-05-17 00:00:00Z (xsd:dateTime)
educated at	University of Huddersfield Linacre College
family name	Lloyd Jones
ORCID iD	wds:Q5622427-71a8448c-4079-956c-cf28-087732722eec
ORCID iD	https://orcid.org/0000-0003-2128-6864
ORCID iD	0000-0003-2128-6864
Gateway to Research person ID	wds:Q5622427-5EF62131-890D-40A7-8E8E-6F9DB1C7C419
Gateway to Research person ID	8E16681F-5AB4-4AEC-B1E8-40ED46301A01
is about of	Guy Lloyd-Jones https://www.wikidata.org/wiki/Special:EntityData/Q5622427 Guy Lloyd-Jones
is author of	New Heteroannulation Reactions ofN-Alkoxybenzamides by Pd(II) Catalyzed C–H Activation Hindered ureas as masked isocyanates: facile carbamoylation of nucleophiles under neutral conditions Switching Pathways: Room-Temperature Neutral Solvolysis and Substitution of Amides Distinct reactivity of Pd(OTs)2: the intermolecular Pd(II)-catalyzed 1,2-carboamination of dienes Pd(II)-catalyzed intermolecular 1,2-diamination of conjugated dienes Selection of boron reagents for Suzuki-Miyaura coupling. Room-temperature palladium-catalyzed C-H activation: ortho-carbonylation of aniline derivatives Structure-based rationale for selectivity in the asymmetric allylic alkylation of cycloalkenyl esters employing the Trost 'Standard Ligand' (TSL): isolation, analysis and alkylation of the monomeric form of the cationic eta(3)-cyclohexenyl complex [ Aryl trifluoroborates in Suzuki-Miyaura coupling: the roles of endogenous aryl boronic acid and fluoride Organotrifluoroborate Hydrolysis: Boronic Acid Release Mechanism and an Acid–Base Paradox in Cross-Coupling The Newman-Kwart rearrangement of O-aryl thiocarbamates: substantial reduction in reaction temperatures through palladium catalysis Transmetalation in the Suzuki-Miyaura coupling: the fork in the trail. Readily accessible, modular, and tuneable BINOL 3,3'-perfluoroalkylsulfones: highly efficient catalysts for enantioselective in-mediated imine allylation

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